LimFlow V-Ceiver

GUDID 00850041730141

Intravascular extraction catheter-snare

Primary Device ID	00850041730141
NIH Device Record Key	0bb5381f-9970-4f96-8684-18ebf1e415a9
Commercial Distribution Status	In Commercial Distribution
Brand Name	LimFlow V-Ceiver
Version Model Number	VC-US-23
Company DUNS	096651686
Company Name	Limflow Inc.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00850041730141 [Primary]

MMX	Device, Percutaneous Retrieval

Steralize Prior To Use	false
Device Is Sterile	true

00850041730004	The LimFlow V-Ceiver is intended for use in the cardiovascular system to manipulate and retrieve
00850041730141	The LimFlow V-Ceiver is intended for use in the cardiovascular system to manipulate and retrieve